# FDA recall Z-2414-2023

> **Abbott Diabetes Care, Inc.** · Class II · device recall initiated 2023-07-12.

## Product

FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System

## Reason for recall

If blood glucose monitoring system users attempt to start a new sensor, when the old sensor wasn't used for the full 14-day wear time, then the reader may display "Incompatible Sensor" message. If users don't have the previous sensor, or FreeStyle Libre 2 app, or the sensor's full wear time hasn't ended, users may be unable to start a new sensor, which could result in no or delayed glucose results

## Distribution

US Nationwide distribution in the states of CA, FL, MI, NY, OH, TX, UT, VA.

## Key facts

- **Recall number:** Z-2414-2023
- **Recalling firm:** Abbott Diabetes Care, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-07-12
- **Report date:** 2023-08-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Alameda, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2414-2023

## Citation

> AI Analytics. FDA recall Z-2414-2023. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2414-2023. Source: US FDA. Licensed CC0.

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